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      Schrodinger’s scat: a critical review of the currently available tiger ( Panthera Tigris) and leopard ( Panthera pardus) specific primers in India, and a novel leopard specific primer

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          Abstract

          Background

          Non-invasive sampling has opened avenues for the genetic study of elusive species, which has contributed significantly to their conservation. Where field based identity of non-invasive sample is ambiguous (e.g. carnivore scats), it is essential to establish identity of the species through molecular approaches. A cost effective procedure to ascertain species identity is to use species specific primers (SSP) for PCR amplification and subsequent resolution through agarose gel electrophoresis. However, SSPs if ill designed can often cross amplify non-target sympatric species. Herein we report the problem of cross amplification with currently published SSPs, which have been used in several recent scientific articles on tigers ( Panthera tigris) and leopards ( Panthera pardus) in India. Since these papers form pioneering research on which future work will be based, an early rectification is required so as to not propagate this error further.

          Results

          We conclusively show cross amplification of three of the four SSPs, in sympatric non-target species like tiger SSP amplifying leopard and striped hyena ( Hyaena hyaena), and leopard SSP amplifying tiger, lion ( Panthera leo persica) and clouded leopard ( Neofelis nebulosa), with the same product size. We develop and test a non-cross-amplifying leopard specific primer pair within the mitochondrial cytochrome b region. We also standardize a duplex PCR method to screen tiger and leopard samples simultaneously in one PCR reaction to reduce cost and time.

          Conclusions

          These findings suggest the importance of an often overlooked preliminary protocol of conclusive identification of species from non-invasive samples. The cross amplification of published primers in conspecifics suggests the need to revisit inferences drawn by earlier work.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12863-016-0344-y) contains supplementary material, which is available to authorized users.

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          Most cited references19

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          Facts from feces revisited.

          Obtaining information on wild mammal populations has been a long-standing logistical problem. However, an array of non-invasive techniques is available, including recently developed molecular genetic techniques for the analysis of feces (molecular scatology). A battery of non-invasive, molecular approaches can be used on feces, which in conjunction with conventional analysis are potentially useful for assesing genetic structure, demography and life history of mammals. Several technical problems reman before large-scale studies of feces can be undertaken productively, but already studies are providing insight into population subdivision, food habits, reproduction, sex ratio and parasitology of free-ranging populations.
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            The expansion of conservation genetics.

            The 'crisis discipline' of conservation biology has voraciously incorporated many technologies to speed up and increase the accuracy of conservation decision-making. Genetic approaches to characterizing endangered species or areas that contain endangered species are prime examples of this. Technical advances in areas such as high-throughput sequencing, microsatellite analysis and non-invasive DNA sampling have led to a much-expanded role for genetics in conservation. Such expansion will allow for more precise conservation decisions to be made and, more importantly, will allow conservation genetics to contribute to area- and landscape-based decision-making processes.
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              On the origin of faeces: morphological versus molecular methods for surveying rare carnivores from their scats

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                Author and article information

                Contributors
                pranay.amrut@gmail.com
                sonu.bsc90@gmail.com
                kolipakam@gmail.com
                singhshweta1090@gmail.com
                qnq@wii.gov.in
                jhalay@wii.gov.in
                Journal
                BMC Genet
                BMC Genet
                BMC Genetics
                BioMed Central (London )
                1471-2156
                9 February 2016
                9 February 2016
                2016
                : 17
                : 37
                Affiliations
                Wildlife Institute of India, Chandrabani, Dehradun, 248001 India
                Author information
                http://orcid.org/0000-0003-3276-1384
                Article
                344
                10.1186/s12863-016-0344-y
                4748499
                26860950
                ae2d102d-7fd2-448b-b020-d50e1ee1889f
                © Maroju et al. 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 2 September 2015
                : 2 February 2016
                Funding
                Funded by: National Tiger Conservation Authority
                Categories
                Methodology Article
                Custom metadata
                © The Author(s) 2015

                Genetics
                species specific primers (ssp),non-invasive genetic sampling,fecal dna,duplex pcr
                Genetics
                species specific primers (ssp), non-invasive genetic sampling, fecal dna, duplex pcr

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